EA201070912A1 - OXIMA DERIVATIVES AS HSP90 INHIBITORS - Google Patents
OXIMA DERIVATIVES AS HSP90 INHIBITORSInfo
- Publication number
- EA201070912A1 EA201070912A1 EA201070912A EA201070912A EA201070912A1 EA 201070912 A1 EA201070912 A1 EA 201070912A1 EA 201070912 A EA201070912 A EA 201070912A EA 201070912 A EA201070912 A EA 201070912A EA 201070912 A1 EA201070912 A1 EA 201070912A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- oxima
- derivatives
- compounds
- hsp90 inhibitors
- present
- Prior art date
Links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/57—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/78—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 2
- C07D239/84—Nitrogen atoms
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- Pain & Pain Management (AREA)
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- Heart & Thoracic Surgery (AREA)
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Abstract
Настоящее изобретение относится к соединениям, ингибирующим HSP90, имеющим формулув которой переменные определены в настоящем описании. Настоящее изобретение также относится к фармацевтическим композициям, наборам и изделиям, включающим такие соединения; способам и промежуточным соединениям, полезным для получения таких соединений; а также способам использования таких соединений.The present invention relates to compounds that inhibit HSP90, having the formula in which the variables are defined in the present description. The present invention also relates to pharmaceutical compositions, kits and articles comprising such compounds; methods and intermediates useful for preparing such compounds; as well as methods for using such compounds.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US2572508P | 2008-02-01 | 2008-02-01 | |
US10159508P | 2008-09-30 | 2008-09-30 | |
PCT/US2009/032728 WO2009097578A1 (en) | 2008-02-01 | 2009-01-30 | Oxim derivatives as hsp90 inhibitors |
Publications (2)
Publication Number | Publication Date |
---|---|
EA201070912A1 true EA201070912A1 (en) | 2011-08-30 |
EA019156B1 EA019156B1 (en) | 2014-01-30 |
Family
ID=40436400
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA201070912A EA019156B1 (en) | 2008-02-01 | 2009-01-30 | Oxim derivatives as hsp90 inhibitors |
Country Status (26)
Country | Link |
---|---|
US (4) | US8071766B2 (en) |
EP (1) | EP2252595B1 (en) |
JP (1) | JP5524084B2 (en) |
KR (1) | KR20100116206A (en) |
CN (1) | CN101983191B (en) |
AR (1) | AR071452A1 (en) |
AU (1) | AU2009208947B2 (en) |
BR (1) | BRPI0906598A2 (en) |
CA (1) | CA2713658C (en) |
CL (1) | CL2009000228A1 (en) |
CR (1) | CR11659A (en) |
DO (1) | DOP2010000236A (en) |
EA (1) | EA019156B1 (en) |
EC (1) | ECSP10010434A (en) |
ES (1) | ES2475206T3 (en) |
GE (1) | GEP20125718B (en) |
IL (1) | IL207227A0 (en) |
MA (1) | MA32104B1 (en) |
MX (1) | MX2010008269A (en) |
MY (1) | MY150596A (en) |
NZ (1) | NZ587207A (en) |
PE (1) | PE20091371A1 (en) |
SG (1) | SG187502A1 (en) |
TW (1) | TW200946531A (en) |
WO (1) | WO2009097578A1 (en) |
ZA (1) | ZA201005435B (en) |
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ES2572263T3 (en) | 2005-10-25 | 2016-05-31 | Shionogi & Co | Dihydrooxazine and tetrahydropyrimidine derivatives as BACE 1 inhibitors |
AR061185A1 (en) | 2006-05-26 | 2008-08-13 | Chugai Pharmaceutical Co Ltd | HETEROCICLICAL COMPOUNDS AS INHIBITORS OF HSP90. PHARMACEUTICAL COMPOSITIONS. |
CL2008000629A1 (en) | 2007-03-01 | 2008-08-29 | Chugai Pharmaceutical Co Ltd | MACROCICLICAL COMPOUNDS DERIVED FROM 6-ARIL-4-MERCAPTO- [1.3.5] TRIAZINA / [1.3] PIRIMIDIN-2-AMINA; PHARMACEUTICAL COMPOSITION, USEFUL IN THE TREATMENT OF CANCER. |
KR20100017255A (en) | 2007-04-24 | 2010-02-16 | 시오노기 앤드 컴파니, 리미티드 | Aminodihydrothiazine derivatives substituted with cyclic groups |
US8653067B2 (en) | 2007-04-24 | 2014-02-18 | Shionogi & Co., Ltd. | Pharmaceutical composition for treating Alzheimer's disease |
GB2449293A (en) * | 2007-05-17 | 2008-11-19 | Evotec | Compounds having Hsp90 inhibitory activity |
GEP20125718B (en) * | 2008-02-01 | 2012-12-25 | Takeda Pharmaceuticals Co | Oxim derivatives as hsp90 inhibitors |
ES2738123T3 (en) | 2008-06-13 | 2020-01-20 | Shionogi & Co | Heterocyclic sulfur-containing derivative that has β-secretase inhibitory activity |
CN102186841A (en) | 2008-10-22 | 2011-09-14 | 盐野义制药株式会社 | 2-aminopyridin-4-one and 2-aminopyridine derivative both having bace1-inhibiting activity |
BR112012013854A2 (en) | 2009-12-11 | 2019-09-24 | Shionogi & Co | oxazine derivatives. |
WO2012057247A1 (en) | 2010-10-29 | 2012-05-03 | 塩野義製薬株式会社 | Fused aminodihydropyrimidine derivative |
CA2816285A1 (en) | 2010-10-29 | 2012-05-03 | Shionogi & Co., Ltd. | Naphthyridine derivative |
TW201247635A (en) | 2011-04-26 | 2012-12-01 | Shionogi & Co | Oxazine derivatives and a pharmaceutical composition for inhibiting BAC1 containing them |
ITTO20111013A1 (en) | 2011-11-03 | 2013-05-04 | Dac Srl | PHARMACEUTICAL COMPOUNDS |
JP2016501827A (en) | 2012-10-24 | 2016-01-21 | 塩野義製薬株式会社 | Dihydrooxazine or oxazepine derivative having BACE1 inhibitory action |
WO2014107655A1 (en) * | 2013-01-07 | 2014-07-10 | St. Jude Children's Research Hospital | Use of small molecule unfolder protein response modulators to treat tumors with active sonic hedgehog (ssh) signaling due to smoothened (smo) mutation |
AU2014228822A1 (en) | 2013-03-15 | 2015-10-01 | Memorial Sloan-Kettering Cancer Center | HSP90-targeted cardiac imaging and therapy |
US9802978B2 (en) | 2013-08-12 | 2017-10-31 | Emory University | Progesterone phosphate analogs and uses related thereto |
CN113521314A (en) | 2014-09-17 | 2021-10-22 | 纪念斯隆-凯特琳癌症中心 | HSP 90-Targeted inflammation and infection imaging and treatment |
US9868738B2 (en) | 2014-09-19 | 2018-01-16 | Merck Sharp & Dohme Corp. | Diazine-fused amidines as BACE inhibitors, compositions, and their use |
CR20200045A (en) | 2016-04-07 | 2020-03-11 | Glaxosmithkline Ip Dev Ltd | Heterocyclic amides useful as protein modulators |
KR20190138871A (en) * | 2017-04-24 | 2019-12-16 | 사무스 테라퓨틱스, 인코포레이티드 | HSP90 Inhibitor Oral Formulations and Related Methods |
US12110286B2 (en) | 2017-05-26 | 2024-10-08 | Cancer Research Technology Limited | Benzimidazolone derived inhibitors of BCL6 |
US20190134219A1 (en) * | 2017-09-15 | 2019-05-09 | Ampersand Biopharmaceuticals, Inc. | Inhibition of spontaneous metastasis via protein inhibitors of cysteine proteases |
CN112568223B (en) * | 2020-04-13 | 2023-04-21 | 辽宁先达农业科学有限公司 | Herbicidal composition, application thereof and herbicide |
CN111671749A (en) * | 2020-06-12 | 2020-09-18 | 重庆医科大学 | Application of dicoumarol in preparation of HBx protein stability inhibitor |
CN112661668B (en) * | 2020-12-31 | 2023-07-28 | 辽宁先达农业科学有限公司 | N-substituted amide compound and preparation method thereof |
CN114259564B (en) * | 2021-11-30 | 2023-03-14 | 清华大学 | Novel use of HSP90 inhibitors for blocking STAT3 mitochondrial transport and for treating asthma |
CN115073458A (en) * | 2022-07-04 | 2022-09-20 | 山东致泰医药技术有限公司 | Preparation method of avibactam sodium |
CN115381816A (en) * | 2022-08-04 | 2022-11-25 | 武汉市金银潭医院(武汉市传染病医院) | Application of VER50589 in preparing medicine for resisting enterovirus 71 |
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